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Reli®

FDA UDI

Class II (US FDA UDI)

by Myco Medical Supplies Inc.

Identity

Trade Name
RELI® FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
Reli® Safety Hypodermic Needle, 21G x 5/8", 100ea/bx, 16bx/cs FDA UDI
Model / Reference
SHN21G6251 FDA UDI
Description
Reli® Safety Hypodermic Needle, 21G x 5/8", 100ea/bx, 16bx/cs FDA UDI

Identifiers

Catalog Number
SHN21G6251 FDA UDI
Primary DI / UDI-DI
00386120011851 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Hypodermic needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 21 Gauge FDA UDI
Length — 0.625 Inch FDA UDI

Category: Hypodermic needle, single-use

Reli® by Myco Medical Supplies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hypodermic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d5c90432-3ca6-4d81-9b3d-268fd59f9d3f 35 fields · synced May 31, 2026